Canonical Allele Identifier: CA2668795868

Gene: EIF2B5

Linked Data

• gnomAD v4: 3-184136927-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184136927T>C , CM000665.2:g.184136927T>C	GRCh38
NC_000003.11:g.183854715T>C , CM000665.1:g.183854715T>C	GRCh37
NC_000003.10:g.185337409T>C	NCBI36
NG_015826.1:g.6906T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432569.2:c.*187T>C	ENSP00000414775.1:n.*187T>C
ENST00000465218.3:n.343+191T>C
ENST00000468748.7:n.303+191T>C
ENST00000471832.2:c.*505T>C	ENSP00000497786.1:n.*505T>C
ENST00000484154.2:n.249T>C
ENST00000491008.6:n.376T>C
ENST00000492226.2:n.317+191T>C
ENST00000492773.6:c.52+191T>C
ENST00000647636.1:c.320+191T>C	ENSP00000497505.1:n.320+191T>C
ENST00000647909.1:c.320+191T>C	ENSP00000498164.1:n.320+191T>C
ENST00000648145.1:c.88+191T>C
ENST00000648189.1:c.70+191T>C
ENST00000648256.1:c.269+191T>C	ENSP00000497356.1:n.269+191T>C
ENST00000648314.1:c.320+191T>C	ENSP00000496920.1:n.320+191T>C
ENST00000648599.1:c.320+191T>C	ENSP00000497159.1:n.320+191T>C
ENST00000648630.1:c.314+191T>C	ENSP00000497887.1:n.314+191T>C
ENST00000648682.1:c.320+191T>C	ENSP00000498185.1:n.320+191T>C
ENST00000648882.1:c.*146+191T>C	ENSP00000497603.1:n.*146+191T>C
ENST00000648890.1:c.320+191T>C	ENSP00000497503.1:n.320+191T>C
ENST00000648915.2:c.320+191T>C MANE Select	ENSP00000497160.1:n.320+191T>C
ENST00000649545.1:c.54+191T>C
ENST00000649688.1:c.320+191T>C	ENSP00000497097.1:n.320+191T>C
ENST00000649814.1:n.369+191T>C
ENST00000650244.1:c.465+191T>C	ENSP00000497227.1:n.465+191T>C
ENST00000650270.1:c.187+191T>C
ENST00000273783.7:c.320+191T>C	ENSP00000273783.3:n.320+191T>C
ENST00000432569.1:c.*187T>C	ENSP00000414775.1:n.*187T>C
ENST00000432982.5:c.245+252T>C
ENST00000444495.1:c.320+191T>C	ENSP00000409142.1:n.320+191T>C
ENST00000471832.1:n.442T>C
ENST00000481054.5:n.321+191T>C
ENST00000491144.5:n.668+191T>C
ENST00000498831.1:n.176+191T>C
NM_003907.2:c.320+191T>C	NP_003898.2:n.320+191T>C
XR_924208.1:n.1271+191T>C
NM_003907.3:c.320+191T>C MANE Select	NP_003898.2:n.320+191T>C
XM_011513266.3:c.-582+191T>C	XP_011511568.1:n.-582+191T>C
XR_001740352.2:n.683+191T>C
XR_001740353.2:n.683+191T>C
XR_924208.2:n.683+191T>C